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Merosin‐deficient congenital muscular dystrophy: neuropathology case reports
The aims of our study were: to present cases of congenital muscular dystrophy (CMD) with deficiency in merosin and the importance of immunohistochemistry in the diagnosis of merosin‐deficient CMD. In four years (1997‐2000), we found three patients with merosin‐deficient CMD, one of them having an un...
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| Izdano u: | J Cell Mol Med |
|---|---|
| Glavni autori: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Blackwell Publishing Ltd
2007
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6745520/ https://ncbi.nlm.nih.gov/pubmed/12067464 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2000.tb00129.x |
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